Package Insert: Information for the Patient
Rosuvastatina Combix 20 mg Film-Coated Tablets
Read this package insert carefully before starting to take this medication, becauseit containsimportant information foryou.
6. Contents of the pack and additional information
Rosuvastatin Combix belongs to a group of medications called statins.
They have prescribed Rosuvastatin Combix because:
Rosuvastatin Combix is used in adults, adolescents, and children aged 6 years or older to treat high cholesterol.
They have indicated that you should take a statin because the changes made to your diet and the increase in physical exercise have not been sufficient to correct your cholesterol levels. You must maintain a diet that helps to reduce cholesterol and continue exercising while on treatment with Rosuvastatin Combix.
Or
A heart attack, cerebral infarction, and other health-related problems may be caused by a disease called atherosclerosis. Atherosclerosis is caused by the formation of fatty deposits in your arteries.
Why is it important to continue taking Rosuvastatin Combix?
Rosuvastatin Combix is used to correct the levels of fatty substances in the blood called lipids, with cholesterol being the most well-known.
There are different types of cholesterol in the blood, bad cholesterol (LDL-C) and good cholesterol (HDL-C).
In most people, high cholesterol levels do not affect how they feel since they do not produce any symptoms. However, if left untreated, fatty deposits can form in the walls of blood vessels, causing them to narrow.
Sometimes, these narrowed vessels can become blocked, preventing blood supply to the heart or brain, causing a heart attack or cerebral infarction. By reducing your cholesterol levels, you can reduce the risk of suffering a heart attack, cerebral infarction, or other health-related problems.
You needto continue taking Rosuvastatin Combix, even if you have already achieved the correct cholesterol levels, as itprevents cholesterol levels from increasing again and forming fatty deposits.However, you should interrupt treatment if your doctor indicates so or if you become pregnant.
Do not take Rosuvastatina Combix
If you find yourself in any of the above situations (or are unsure), please consult your doctor again.
Also, do not take the highest dose of Rosuvastatina 40 mg
If you find yourself in any of the above situations (or are unsure),please consult your doctor again.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Rosuvastatina Combix:
Follow exactly the administration instructions of this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
Usual doses in adults
If you are taking Rosuvastatina Combix for high cholesterol levels:
Starting dose
Your treatment with Rosuvastatina Combix should start witha dose of 5 mg or 10 mg, even if you have taken a higher dose of another statin previously.
The choice of starting dose will depend on:
Check with your doctor or pharmacist which is the best starting dose of Rosuvastatina Combix for you.
Your doctor may decide to start treatment with the lowest dose (5 mg):
Dose increase and maximum daily dose
Your doctor may decide to increase your dose. This is to ensure you are taking the right dose of rosuvastatin for you. If you started with a dose of 5 mg, your doctor may decide to double the dose to 10 mg, then to 20 mg and later to 40 mg, if necessary. If you started with a dose of 10 mg, your doctor may decide to double the dose to 20 mg and then to 40 mg, if necessary. There will be a four-week interval between each dose adjustment.
The maximum daily dose of rosuvastatin is 40 mg. This dose is only for patients with high cholesterol levels and a high risk of having a heart attack or stroke, whose cholesterol levels do not decrease enough with 20 mg.
If you are taking rosuvastatin to reduce the risk of having a heart attack, a stroke or related health problems:
The recommended dose is 20 mg per day. However, your doctor may decide to use a lower dose if you have any of the factors mentioned earlier.
Use in children and adolescents aged 6-17 years
The usual recommended starting dose is 5 mg. Your doctor may increase your dose to reach the right dose of rosuvastatin to treat your condition. The maximum daily recommended dose of rosuvastatin is 10 mg for children aged 6-9 years and 20 mg for children aged 10-17 years. Take the dose indicated by your doctor once a day.Do notadminister the 40 mg tablets of rosuvastatin to children.
Swallowing the tablets
Swallow each tablet whole with water.
Take Rosuvastatina Combix once a day. You can take it at any time of the day with or without food.
Try to take the tablets at the same time every day. This will help you remember to take them.
Regular cholesterol checks
It is essential that you attend your doctor regularly for cholesterol checks, to ensure that your cholesterol levels have normalized and remain at appropriate levels.
Your doctor may decide to increase your dose so that you are taking the right dose of rosuvastatin for you.
If you take more Rosuvastatina Combix than you should
Contact your doctor or nearest hospital for advice.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you enter a hospital or receive treatment for another condition, inform the healthcare staff that you are taking Rosuvastatina Combix.
If you forget to take Rosuvastatina Combix
Do not worry, simply take the next scheduled dose at the planned time.
Do not take a double dose to compensate for a missed dose.
If you interrupt treatment with Rosuvastatina Combix
Consult your doctor if you want to stop taking rosuvastatin. Your cholesterol levels may increase again if you stop taking rosuvastatin.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
It is essential that you know which side effects may occur. They are usually mild and disappear within a short period of time.
Stop taking Rosuvastatina Combix and seek immediate medical attentionif you experience any of the following allergic reactions:
Also, stop taking this medicine and consult your doctor immediately if you experience:
Frequent side effects (may affect up to 1 in 10 people)
Rare side effects (may affect up to 1 in 100 people)
Very rare side effects (may affect up to 1 in 10,000 people)
Side effects of unknown frequency (cannot be estimated from available data) that may include
Consult your doctor if you experience weakness in the arms or legs that worsens after periods of activity, double vision, eyelid drooping, difficulty swallowing, or difficulty breathing.
Reporting side effects:
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medicines at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medicines. By doing so, you will help protect the environment.
Composition of Rosuvastatina Combix
Tablet core: Lactose monohydrate, microcrystalline cellulose (E460i), crospovidone, meglumine, magnesium stearate (E470b).
Coating: Opadry II 33K540005 pink: Hypromellose (E464), lactose monohydrate, titanium dioxide (E171), triacetin, aluminium lake yellow-orange S (E110), aluminium lake red allura AC (E129) and aluminium carmine of indigo (E132).
Appearance of the product and content of the container
Film-coated tablets, pink in color, round, biconvex, with the engraving “20” on one face and smooth on the other.
Aluminium/Aluminium blisters with desiccant.
Packaging of 28 tablets.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Laboratorios Combix, S.L.U.
C/ Badajoz 2, Edificio 2
28223 Pozuelo de Alarcón (Madrid)
Spain
Responsible for manufacturing
Zydus France
ZAC Les Hautes Patures
Parc d'activités des Peupliers
25 Rue des Peupliers
92000 Nanterre
France
or
Centre Spécialités Pharmaceutiques
ZAC des Suzots
35 rue de la Chapelle
63450 Saint Amant Tallende
France
Last review date of this leaflet: April 2023
The detailed and updated information of this medicine is available on the website of the Spanish Agency of Medicaments and Health Products (AEMPS)http://www.aemps.gob.es.
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